- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT05032911
Sensorimotor Control in People With and Without Neck Pain
Analysis of Sensorimotor Control in People With and Without Neck Pain Using Inertial Sensor Technology: Study Protocol for a Longitudinal Prospective Observational Study
This is a descriptive, observational, longitudinal, prospective study consecutively enrolling patients with non-specific neck pain and age-matched asymptomatic participants.
The investigators will register sensorimotor control variables, including active range of motion, movement speed, acceleration, smoothness of motion, head repositioning accuracy and motion coupling patterns. These variables will be recorded by means of Inertial Measurement Unit (IMU) sensors during the following tests consecutively performed in two measuring sessions separated by 12 months: (a) kinematics of planar movements, (b) kinematics of the craniocervical flexion movement, (c) kinematics during functional tasks and (d) kinematics of task-oriented neck movements in response to visual targets.
Studieöversikt
Status
Betingelser
Intervention / Behandling
Studietyp
Inskrivning (Förväntat)
Kontakter och platser
Studiekontakt
- Namn: Aitor Martin Pintado Zugasti, PhD
- Telefonnummer: 14691 91 3724700
- E-post: martinpintado@ceu.es
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Testmetod
Studera befolkning
Beskrivning
Inclusion Criteria:
- Population aged between 18 and 65 years old
Exclusion Criteria:
- Visual impairment not corrected by the use of glasses/contact lenses
- Migraine headache
- Complex regional syndrome
- Previous surgeries in the neck and/or head region
- Sensory and/or vestibular alterations, (f) Otogenic or idiopathic vertigo/dizziness
- Presence of tumors in the craniocervical region
- Previous fracture in the head or neck region
- Osseous deformities in the thoracic, cervical or cranial region
Studieplan
Hur är studien utformad?
Designdetaljer
Kohorter och interventioner
Grupp / Kohort |
Intervention / Behandling |
---|---|
Asymptomatic participants
Asymptomatic subjects should not present any pain in the cervical region during the last 3 months and no previous treatment for neck pain in order to be included in the study.
|
Inertial Measurement Unit (IMU) sensors will measure sensorimotor control variables including active range of motion, movement speed, acceleration, smoothness of motion, head repositioning accuracy and motion coupling patterns
|
Neck pain patients
Patients with neck pain should have an intensity of pain of at least 3 points out of 10 on a Visual Analog Scale and a neck pain duration of at least 3 months of evolution.
Neck pain could be from nonspecific mechanical origin, associated with whiplash or with a previous medical diagnosis of degenerative or inflammatory alterations of the cervical spine, associated or not with headache and pain in the shoulder region or the upper limb.
|
Inertial Measurement Unit (IMU) sensors will measure sensorimotor control variables including active range of motion, movement speed, acceleration, smoothness of motion, head repositioning accuracy and motion coupling patterns
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
---|---|---|
Active range of motion
Tidsram: 1 year
|
Expressed as an angular displacement (°) in 3 full-movements (flexion-extension, lateral flexion and rotation)
|
1 year
|
Movement speed
Tidsram: 1 year
|
Expressed as angular velocity (°/sec) in 3 full-movements (flexion-extension, lateral flexion and rotation)
|
1 year
|
Smoothness of motion
Tidsram: 1 year
|
expressed as movement jerk (º/sec3)
|
1 year
|
Head repositioning accuracy
Tidsram: 1 year
|
Calculated as the repositioning error considering the difference between the neutral starting position and the following positions reached after the performance of any of the movements
|
1 year
|
Motion coupling patterns
Tidsram: 1 year
|
Calculated as the angular displacement occurring in a different anatomical plane to the one that is being tested for each of the planar movements
|
1 year
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
---|---|---|
Physical activity level
Tidsram: 1 year
|
Measured using the short version of the International Physical Activity Questionnaire (IPAQ).
The score of the scale is expressed in MET level x minutes of activity/day x days per week.
Levels of 3.3 METs are considered light, 4.0 METs are moderate and 8.0 METs are vigorous.
|
1 year
|
Fear of movement and injury
Tidsram: 1 year
|
Measured using the Tampa Scale for Kinesiophobia (TSK-11).
It consists of 11 questions scored from 1 to 4. Therefore, a score of 11 is the lowest possible level of kinesiphobia, while 44 is the highest.
|
1 year
|
Pain-related fear-avoidance
Tidsram: 1 year
|
Measured using the Fear Avoidance Components Scale (FACS).
It has 20 itemsmeasured on a 6-point Likert scale for total possible score of 100 and the lowest possible score of 0. Higher scores indicate higher levels of fear avoidance.
|
1 year
|
Samarbetspartners och utredare
Sponsor
Publikationer och användbara länkar
Studieavstämningsdatum
Studera stora datum
Studiestart (Förväntat)
Primärt slutförande (Förväntat)
Avslutad studie (Förväntat)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- CEU-023
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